Canonical Allele Identifier: CA1300460529

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329620A= , CM000664.2:g.156329620A=	GRCh38
NC_000002.11:g.157186132A= , CM000664.1:g.157186132A=	GRCh37
NC_000002.10:g.156894378A=	NCBI36
NG_011821.1:g.8156T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.378T=	ENSP00000388120.2:p.Ser126=
ENST00000700228.1:c.438T=	ENSP00000514865.1:p.Ser146=
ENST00000700231.1:c.567T=	ENSP00000514868.1:p.Ser189=
ENST00000339562.9:c.567T= MANE Select	ENSP00000344479.4:p.Ser189=
ENST00000675870.1:c.378T=	ENSP00000502739.1:p.Ser126=
ENST00000339562.8:c.567T=	ENSP00000344479.4:p.Ser189=
ENST00000406048.2:c.208+294T=
ENST00000409108.6:c.567T=	ENSP00000386993.2:p.Ser189=
ENST00000409572.5:c.567T=	ENSP00000386747.1:p.Ser189=
ENST00000417764.5:c.378T=	ENSP00000415632.1:p.Ser126=
ENST00000417972.5:c.378T=	ENSP00000394671.1:p.Ser126=
ENST00000424077.1:c.567T=	ENSP00000406808.1:p.Ser189=
ENST00000426264.5:c.378T=	ENSP00000389986.1:p.Ser126=
ENST00000429376.5:c.378T=	ENSP00000410952.1:p.Ser126=
NM_006186.3:c.567T=	NP_006177.1:p.Ser189=
XM_005246621.2:c.600T=	XP_005246678.1:p.Ser200=
XM_005246622.2:c.378T=	XP_005246679.1:p.Ser126=
XM_005246623.1:c.378T=	XP_005246680.1:p.Ser126=
XM_006712553.2:c.600T=	XP_006712616.1:p.Ser200=
XM_011511246.1:c.600T=	XP_011509548.1:p.Ser200=
XR_427087.2:n.2773T=
NM_173173.2:c.378T=	NP_775265.1:p.Ser126=
XM_005246621.4:c.600T=	XP_005246678.1:p.Ser200=
XM_006712553.4:c.600T=	XP_006712616.1:p.Ser200=
XM_011511246.2:c.600T=	XP_011509548.1:p.Ser200=
XM_017004219.2:c.567T=	XP_016859708.1:p.Ser189=
XM_017004220.2:c.567T=	XP_016859709.1:p.Ser189=
XR_001738751.2:n.935T=
XR_001738752.2:n.757T=
XR_427087.4:n.814T=
NM_006186.4:c.567T= MANE Select	NP_006177.1:p.Ser189=
NM_173173.3:c.378T=	NP_775265.1:p.Ser126=